The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Glutaminolysis and Fumarate Accumulation Integrate Immunometabolic and Epigenetic Programs in Trained Immunity
Open accessAbstract
Induction of trained immunity (innate immune memory) is mediated by activation of immune and metabolic pathways that result in epigenetic rewiring of cellular functional programs. Through network-level integration of transcriptomics and metabolomics data, we identify glycolysis, glutaminolysis, and the cholesterol synthesis pathway as indispensable for the induction of trained immunity by β-glucan in monocytes. Accumulation of fumarate, due to glutamine replenishment of the TCA cycle, integrates immune and metabolic circuits to induce monocyte epigenetic reprogramming by inhibiting KDM5 histone demethylases. Furthermore, fumarate itself induced an epigenetic program similar to β-glucan-induced trained immunity. In line with this, inhibition of glutaminolysis and cholesterol synthesis in mice reduced the induction of trained immunity by β-glucan. Identification of the metabolic pathways leading to induction of trained immunity contributes to our understanding of innate immune memory and opens new therapeutic avenues.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Fumarate was shown to cause succination of the mitochondrial aconitase, ACO2, leading to an additional truncation of the TCA cycle86”
From Coupling Krebs cycle metabolites to signalling in immunity and cancer (2018) · cites this paper as [86]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Succinate is an inflammatory signal that induces IL-1β through HIF-1α
Tannahill, G. M., Curtis, A. M., Adamik, J., Palsson-McDermott, E. M., McGettrick, A. F., Goel, G., Frezza, C., Bernard, N. J., Kelly, B., Foley, N. H., et al. (2013) · Nature · doi:10.1038/nature11986 · Cited by 4,176 · cited 1×
“Citric acid cycle metabolites (e.g., fumarate and succinate) have previously been reported to regulate HIF1a stabilization by inhibiting hydroxylation and therefore stabilizing HIF1a (Koi- vunen et al., 2007; Tannahill et al., 2013).”
BackgroundSelf-citationCaspi, R., Billington, R., Ferrer, L., Foerster, H., Fulcher, C. A., Keseler, I. M., Kothari, A., Krummenacker, M., Latendresse, M., Mueller, L. A., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1164 · Cited by 3,395
Trained immunity: A program of innate immune memory in health and– disease
Netea, M. G., Joosten, L. A. B., Latz, E., Mills, K. H. G., Natoli, G., Stunnenberg, H. G., O’Neill, L. A. J., & Xavier, R. J. (2016) · Science · doi:10.1126/science.aaf1098 · Cited by 2,768
Self-citationMetaboAnalyst 3.0—making metabolomics more meaningful
Xia, J., Sinelnikov, I. V., Han, B., & Wishart, D. S. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv380 · Cited by 2,680
mTOR- and HIF-1α–mediated aerobic glycolysis as metabolic basis for trained immunity
Cheng, S.-C., Quintin, J., Cramer, R. A., Shepardson, K. M., Saeed, S., Kumar, V., Giamarellos-Bourboulis, E. J., Martens, J. H. A., Rao, N. A., Aghajanirefah, A., et al. (2014) · Science · doi:10.1126/science.1250684 · Cited by 2,224
Self-citationIDH mutation impairs histone demethylation and results in a block to cell differentiation
Lu, C., Ward, P. S., Kapoor, G. S., Rohle, D., Turcan, S., Abdel-Wahab, O., Edwards, C. R., Khanin, R., Figueroa, M. E., Melnick, A., et al. (2012) · Nature · doi:10.1038/nature10860 · Cited by 1,985
Epigenetic programming of monocyte-to-macrophage differentiation and trained innate immunity
Saeed, S., Quintin, J., Kerstens, H. H. D., Rao, N. A., Aghajanirefah, A., Matarese, F., Cheng, S.-C., Ratter, J., Berentsen, K., van der Ent, M. A., et al. (2014) · Science · doi:10.1126/science.1251086 · Cited by 1,761
Self-citationTrained Immunity: A Memory for Innate Host Defense
Netea, M. G., Quintin, J., & van der Meer, J. W. M. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.04.006 · Cited by 1,760
Self-citationKleinnijenhuis, J., Quintin, J., Preijers, F., Joosten, L. A. B., Ifrim, D. C., Saeed, S., Jacobs, C., van Loenhout, J., de Jong, D., Stunnenberg, H. G., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202870109 · Cited by 1,728
Self-citationHypoxia-Inducible Factor-1 (HIF-1)
Ke, Q., & Costa, M. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.027029 · Cited by 1,690
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 927
Sepsis Induces a Long-Lasting State of Trained Immunity in Bone Marrow Monocytes
Bomans, K., Schenz, J., Sztwiertnia, I., Schaack, D., Weigand, M. A., & Uhle, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02685 · Cited by 73
IL-1 family cytokines as drivers and inhibitors of trained immunity
Teufel, L. U., Arts, R. J. W., Netea, M. G., Dinarello, C. A., & Joosten, L. A. B. (2021) · Cytokine · doi:10.1016/j.cyto.2021.155773 · Cited by 73
Self-citationMevalonate Metabolism in Immuno-Oncology
Gruenbacher, G., & Thurnher, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01714 · Cited by 76
OxLDL-mediated immunologic memory in endothelial cells
Sohrabi, Y., Lagache, S. M. M., Voges, V. C., Semo, D., Sonntag, G., Hanemann, I., Kahles, F., Waltenberger, J. L., & Findeisen, H. M. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.07.006 · Cited by 69
Trained immunity as a novel therapeutic strategy
Mourits, V. P., Wijkmans, J. C., Joosten, L. A. B., & Netea, M. G. (2018) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2018.04.007 · Cited by 69
Self-citationHorneck Johnston, C. J. H., Ledwith, A. E., Lundahl, M. L. E., Charles-Messance, H., Hackett, E. E., O’Shaughnessy, S. D., Clegg, J., Prendeville, H., McGrath, J. P., Walsh, A. M., et al. (2024) · iScience · doi:10.1016/j.isci.2024.109030 · Cited by 67
Seufert, A. L., Hickman, J. W., Traxler, S. K., Peterson, R. M., Waugh, T. A., Lashley, S. J., Shulzhenko, N., Napier, R. J., & Napier, B. A. (2022) · eLife · doi:10.7554/elife.76744 · Cited by 72
The emerging role for metabolism in fueling neutrophilic inflammation
Morrison, T., Watts, E., Sadiku, P., & Walmsley, S. R. (2022) · Immunological Reviews · doi:10.1111/imr.13157 · Cited by 67
Trained innate immunity: Concept, nomenclature, and future perspectives
Netea, M. G., & Joosten, L. A. B. (2024) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2024.09.005 · Cited by 71
Self-citationHoogeveen, R. M., Nahrendorf, M., Riksen, N. P., Netea, M. G., de Winther, M. P. J., Lutgens, E., Nordestgaard, B. G., Neidhart, M., Stroes, E. S. G., Catapano, A. L., et al. (2017) · European Heart Journal · doi:10.1093/eurheartj/ehx581 · Cited by 65
Self-citationLee, M.-C., Achuthan, A. A., Souza, D. P. D., Lupancu, T. J., Binger, K. J., Lee, M. K. S., Xu, Y., McConville, M. J., de Weerd, N. A., Dragoljevic, D., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110719 · Cited by 64
Cardiac macrophages and emerging roles for their metabolism after myocardial infarction
Thorp, E. B. (2023) · Journal of Clinical Investigation · doi:10.1172/jci171953 · Cited by 66
Innate Immunomodulation in Food Animals: Evidence for Trained Immunity?
Byrne, K. A., Loving, C. L., & McGill, J. L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01099 · Cited by 65
The Causes and Consequences of Trained Immunity in Myeloid Cells
Bhargavi, G., & Subbian, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1365127 · Cited by 62
Glycolysis in Innate Immune Cells Contributes to Autoimmunity
Xu, Y., Chen, Y., Zhang, X., Ma, J., Liu, Y., Cui, L., & Wang, F. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.920029 · Cited by 64
Tricarboxylic acid cycle metabolites in the control of macrophage activation and effector phenotypes
Noe, J. T., & Mitchell, R. A. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ru1218-496r · Cited by 63
Bakker, N. V. T., & Pearce, E. J. (2020) · Immunological Reviews · doi:10.1111/imr.12848 · Cited by 62
Immunometabolism of tumor-associated macrophages: A therapeutic perspective
Karimova, A. F., Khalitova, A. R., Suezov, R. V., Markov, N., Mukhamedshina, Y. O., Rizvanov, A. A., Huber, M., Simon, H., & Brichkina, A. I. (2025) · European Journal of Cancer · doi:10.1016/j.ejca.2025.115332 · Cited by 65
Janbon, G., Quintin, J., Lanternier, F., & d’Enfert, C. (2019) · Microbes and Infection · doi:10.1016/j.micinf.2019.06.011 · Cited by 66
Trained Immunity: Linking Obesity and Cardiovascular Disease across the Life-Course?
Bekkering, S., Saner, C. C. S., Riksen, N. P., Netea, M. G., Sabin, M. A., Saffery, R., Stienstra, R., & Burgner, D. P. (2020) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2020.01.008 · Cited by 60
Self-citationEpigenetics in susceptibility, progression, and diagnosis of periodontitis
Suzuki, S., & Yamada, S. (2022) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2022.06.001 · Cited by 61
From structure to function – Ligand recognition by myeloid C-type lectin receptors
Fischer, S., Stegmann, F., Gnanapragassam, V. S., & Lepenies, B. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.10.019 · Cited by 65
Glutarate regulates T cell metabolism and anti-tumour immunity
Minogue, E., Cunha, P. P., Wadsworth, B. J., Grice, G. L., Sah‐Teli, S. K., Hughes, R. J. F., Bargiela, D., Quaranta, A., Zurita, J., Antrobus, R., et al. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00855-2 · Cited by 60
Histone Deacetylation Inhibitors as Therapy Concept in Sepsis
von Knethen, A., & Brüne, B. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20020346 · Cited by 60
Innate immune memory in inflammatory arthritis
Jeljeli, M. M., & Adamopoulos, I. E. (2023) · Nature Reviews Rheumatology · doi:10.1038/s41584-023-01009-0 · Cited by 60
Candida albicans β-Glucan Differentiates Human Monocytes Into a Specific Subset of Macrophages
Leonhardt, J., Größe, S., Marx, C., Siwczak, F., Stengel, S., Bruns, T., Bauer, R., Kiehntopf, M., Williams, D. L., Wang, Z., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02818 · Cited by 59
Self-citationCentral metabolic interactions of immune cells and microbes: prospects for defeating infections
Traven, A., & Naderer, T. (2019) · EMBO Reports · doi:10.15252/embr.201947995 · Cited by 60
Adaptive innate immunity or innate adaptive immunity?
Černý, J., & Střı́ž, I. (2019) · Clinical Science · doi:10.1042/cs20180548 · Cited by 59
Targeting immunometabolism in host defence against Mycobacterium tuberculosis
Sheedy, F. J., & Divangahi, M. (2020) · Immunology · doi:10.1111/imm.13276 · Cited by 62
Mitochondria orchestrate macrophage effector functions in atherosclerosis
Dumont, A., Lee, M., Barouillet, T., Murphy, A. J., & Yvan‐Charvet, L. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100922 · Cited by 60
Fumarate hydratase as a metabolic regulator of immunity
Peace, C. G., O’Carroll, S. M., & O'Neill, L. A. J. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.10.005 · Cited by 61
Self-citationInflammageing, a targetable pathway for preventing cardiovascular diseases
Aranda, J. F., Ramírez, C. M., & Mittelbrunn, M. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae240 · Cited by 64
Trained Immunity: An Overview and the Impact on COVID-19
Brueggeman, J., Zhao, J., Schank, M., Yao, Z. Q., & Moorman, J. P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.837524 · Cited by 58
Training vs. Tolerance: The Yin/Yang of the Innate Immune System
Lajqi, T., Köstlin‐Gille, N., Bauer, R., Zarogiannis, S. G., Lajqi, E., Ajeti, V., Dietz, S., Kranig, S. A., Rühle, J., Demaj, A., et al. (2023) · Biomedicines · doi:10.3390/biomedicines11030766 · Cited by 60
SDHA gain-of-function engages inflammatory mitochondrial retrograde signaling via KEAP1–Nrf2
Burgener-Gasser, A.-V., Bantug, G. R., Meyer, B. J., Higgins, R., Ghosh, A., Bignucolo, O., Ma, E. H., Loeliger, J., Unterstab, G., Geigges, M., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0482-2 · Cited by 57
Systemic Immuno-metabolic alterations in chronic obstructive pulmonary disease (COPD)
Agarwal, A., Kadam, S., Brahme, A., Agrawal, M. Y., Apte, K. K., Narke, G., Kekan, K., Madas, S. J., & Salvi, S. S. (2019) · Respiratory Research · doi:10.1186/s12931-019-1139-2 · Cited by 56
Metabolic regulation in the immune response to cancer
Wu, Q., Yu, X., Li, J., Sun, S., & Tu, Y. (2021) · 癌症:英文版 · doi:10.1002/cac2.12182 · Cited by 57
Dendritic cells in sepsis: Potential immunoregulatory cells with therapeutic potential
Kumar, V. (2018) · Molecular Immunology · doi:10.1016/j.molimm.2018.07.007 · Cited by 57
Li, T., Kong, L., Li, X., Wu, S., Attri, K. S., Li, Y., Gong, W., Zhao, B. L., Li, L., Herring, L. E., et al. (2021) · Nature Microbiology · doi:10.1038/s41564-020-00843-2 · Cited by 56
RetractedMetabolic regulation of epigenetic remodeling in immune cells
Britt, E. C., John, S. V., Locasale, J. W., & Fan, J. (2020) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2019.12.008 · Cited by 54
Consequences of Metabolic Interactions during Staphylococcus aureus Infection
Lung, T. W. F., & Prince, A. S. (2020) · Toxins · doi:10.3390/toxins12090581 · Cited by 57
Trained immunity: A Yin‐Yang balance
Hu, Z., Lu, S., Lowrie, D. B., & Fan, X. (2022) · MedComm · doi:10.1002/mco2.121 · Cited by 55
Pulmonary Pathogens Adapt to Immune Signaling Metabolites in the Airway
Riquelme, S. A., Lung, T. W. F., & Prince, A. S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00385 · Cited by 53
Arifuzzaman, S., Khatun, M. R., & Khatun, R. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110392 · Cited by 55
Cox, D. J., Coleman, A. M., Gogan, K. M., Phelan, J. J., Maoldomhnaigh, C. Ó., Dunne, P. J., Basdeo, S. A., & Keane, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01609 · Cited by 53
An integrative genomics approach identifies KDM4 as a modulator of trained immunity
Moorlag, S. J. C. F. M., Matzaraki, V., van Puffelen, J. H., van der Heijden, C. D. C. C., Keating, S., Groh, L. A., Röring, R. J., Bakker, O. B., Mourits, V. P., Koeken, V. A. C. M., et al. (2021) · European Journal of Immunology · doi:10.1002/eji.202149577 · Cited by 56
Self-citationRole of Glutamine Metabolism in Host Defense Against Mycobacterium tuberculosis Infection
Koeken, V. A. C. M., Lachmandas, E., Riza, A. L., Matzaraki, V., Li, Y., Kumar, V., Oosting, M., Joosten, L. A. B., Netea, M. G., & van Crevel, R. (2018) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiy709 · Cited by 52
Self-citationInnate immune memory in cardiometabolic disease
Bahrar, H., Bekkering, S., Stienstra, R., Netea, M. G., & Riksen, N. P. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvad030 · Cited by 53
Self-citationTheobald, H., Bejarano, D. A., Katzmarski, N., Haub, J., Schulte-Schrepping, J., Yu, J., Bassler, K. E., Ament, A. L., Osei-Sarpong, C., Piattini, F., et al. (2024) · Nature Immunology · doi:10.1038/s41590-024-01830-z · Cited by 54
Self-citationImmunometabolism of Phagocytes and Relationships to Cardiac Repair
Zhang, S., Bories, G. F. P., Lantz, C. W., Emmons, R., Becker, A., Liu, E., Abecassis, M. M., Yvan‐Charvet, L., & Thorp, E. B. (2019) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2019.00042 · Cited by 54
A molecular atlas of innate immunity to adjuvanted and live attenuated vaccines, in mice
Lee, A. W. Q., Scott, M. K. D., Wimmers, F., Arunachalam, P. S., Luo, W., Fox, C. B., Tomai, M. A., Khatri, P., & Pulendran, B. (2022) · Nature Communications · doi:10.1038/s41467-022-28197-9 · Cited by 52
Trained Innate Immunity and Its Implications for Mucosal Immunity and Inflammation
Hajishengallis, G., Li, X., Mitroulis, I., & Chavakis, T. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-28524-1_2 · Cited by 55
Crosstalk Between Staphylococcus aureus and Innate Immunity: Focus on Immunometabolism
Horn, C. M., & Kielian, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.621750 · Cited by 53
Zhai, X., Liu, K., Fang, H., Zhang, Q., Gao, X., Liu, F., Zhou, S., Wang, X., Niu, Y., Hong, Y., et al. (2021) · Science Advances · doi:10.1126/sciadv.abk0490 · Cited by 53
Lajqi, T., Köstlin‐Gille, N., Hillmer, S., Braun, M., Kranig, S. A., Dietz, S., Krause, C., Rühle, J., Frommhold, D., Pöschl, J. M. B., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10020442 · Cited by 53
Trained Immunity Contribution to Autoimmune and Inflammatory Disorders
Funes, S. C., Ríos, M., Fernández‐Fierro, A., Genaro, M. S. D., & Kalergis, A. M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.868343 · Cited by 53
Guo, Z., Wang, L., Liu, H., & Xie, Y. (2022) · Cells · doi:10.3390/cells11244072 · Cited by 53
Endotoxin tolerance and trained immunity: breaking down immunological memory barriers
López‐Collazo, E., & del Fresno, C. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1393283 · Cited by 54
Mills, T., Kain, B. N., Burchill, M. A., Danis, E. P., Lucas, E. D., Culp‐Hill, R., Cowan, C. M., Schleicher, W. E., Patel, S. B., Tran, B. T., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.09.010 · Cited by 52
Hypothesis: stimulation of trained immunity as adjunctive immunotherapy in cancer
Netea, M. G., Joosten, L. A. B., & van der Meer, J. W. M. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.5ri0217-064rr · Cited by 53
Self-citationHypoxia-inducible factor-1α regulation of myeloid cells
Stothers, C. L., Luan, L., Fensterheim, B. A., & Bohannon, J. K. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1710-1 · Cited by 52
Metabolic substrate utilization in stress-induced immune cells
Zhang, X., Zink, F., Hezel, F., Vogt, J. A., Wachter, U. A., Wepler, M., Loconte, M., Kranz, C., Hellmann, A., Mizaikoff, B., et al. (2020) · Intensive Care Medicine Experimental · doi:10.1186/s40635-020-00316-0 · Cited by 52
Dooming Phagocyte Responses: Inflammatory Effects of Endogenous Oxidized Phospholipids
Gioia, M. D., & Zanoni, I. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.626842 · Cited by 53
Nature versus Number: Monocytes in Cardiovascular Disease
Williams, H., Mack, C. D., Li, S., Fletcher, J., & Medbury, H. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179119 · Cited by 50
Plasma metabolome predicts trained immunity responses after antituberculosis BCG vaccination
Koeken, V. A. C. M., Qi, C., Mourits, V. P., de Bree, L. C. J., Moorlag, S. J. C. F. M., Sonawane, V., Lemmers, H., Dijkstra, H., Joosten, L. A. B., van Laarhoven, A., et al. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001765 · Cited by 50
Self-citationFoxp3 confers long-term efficacy of chimeric antigen receptor-T cells via metabolic reprogramming
Niu, C., Wei, H., Pan, X., Wang, Y., Song, H., Li, C., Qie, J., Qian, J., Mo, S., Zheng, W., et al. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.04.008 · Cited by 49
Altered Cellular Metabolism Drives Trained Immunity
Sohrabi, Y., Godfrey, R., & Findeisen, H. M. (2018) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2018.03.012 · Cited by 51
Fuchs, A. L., Schiller, S. M., Keegan, W. J., Ammons, M. C. B., Eilers, B. J., Tripet, B., & Copié, V. (2019) · Metabolites · doi:10.3390/metabo9110248 · Cited by 51
Bharadwaj, S., Singh, M. V., Kirtipal, N., & Kang, S. G. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.627842 · Cited by 50
Glutathione Metabolism Contributes to the Induction of Trained Immunity
Ferreira, A. V., Koeken, V. A. C. M., Matzaraki, V., Kostidis, S., Alarcon-Barrera, J. C., de Bree, L. C. J., Moorlag, S. J. C. F. M., Mourits, V. P., Novakovic, B., Giera, M. A., et al. (2021) · Cells · doi:10.3390/cells10050971 · Cited by 52
Self-citationImmune Memory in Aging: a Wide Perspective Covering Microbiota, Brain, Metabolism, and Epigenetics
Bulut, O. P., Kılıç, G., & Domínguez‐Andrés, J. (2021) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-021-08905-x · Cited by 50
Wang, Y., Wang, X., Luu, L. D. W., Chen, S., Fu, J. X., Wang, S., Huang, X., Wang, L., Zhou, X., Chen, X., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.848961 · Cited by 48
Self-citationKong, E., Li, Y., Deng, M., Tong, H., Yang, M., Li, J., Feng, X., & Yuan, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.861290 · Cited by 48
The Role of Amino Acids in Tuberculosis Infection: A Literature Review
Amalia, F. I., Syamsunarno, M. R. A. A., Triatin, R. D., Fatimah, S. N., Chaidir, L., & Achmad, T. H. (2022) · Metabolites · doi:10.3390/metabo12100933 · Cited by 48
Kobayashi, T., Nguyen-Tien, D., Sorimachi, Y., Sugiura, Y., Suzuki, T., Karyu, H., Shimabukuro-Demoto, S., Uemura, T., Okamura, T., Taguchi, T., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2100295118 · Cited by 49
Epigenetics: An opportunity to shape innate and adaptive immune responses
Liotti, A., Ferrara, A. L., Loffredo, S., Galdiero, M. R., Varricchi, G., Rella, F. D., Maniscalco, G. T., Belardo, M., Vastano, R., Prencipe, R., et al. (2022) · Immunology · doi:10.1111/imm.13571 · Cited by 50
Exploring Non-Metabolic Functions of Glycolytic Enzymes in Immunity
Seki, S. M., & Gaultier, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01549 · Cited by 49
Grondman, I., Arts, R. J. W., Koch, R. M., Leijte, G. P., Gerretsen, J., Bruse, N., Kempkes, R. W. M., ter Horst, R., Kox, M., Pickkers, P., et al. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.5hi0119-018r · Cited by 48
Self-citationThe double-sided effects of Mycobacterium Bovis bacillus Calmette–Guérin vaccine
Li, J., Zhan, L., & Qin, C. (2021) · npj Vaccines · doi:10.1038/s41541-020-00278-0 · Cited by 48
Cell-specific epigenetic changes in atherosclerosis
Khan, A. W., Paneni, F., & Jandeleit-Dahm, K. A. M. (2021) · Clinical Science · doi:10.1042/cs20201066 · Cited by 46
T cell-based cancer immunotherapy: opportunities and challenges
Ma, K., Xu, Y., Cheng, H., Tang, K., Ma, J., & Huang, B. (2025) · 中国科学通报:英文版 · doi:10.1016/j.scib.2025.03.054 · Cited by 47
Harnessing the Potential of Multiomics Studies for Precision Medicine in Infectious Disease
Ward, R., Aghaeepour, N., Bhattacharyya, R. P., Clish, C. B., Gaudilliere, B. L., Hacohen, N., Mansour, M. K., Mudd, P. A., Pasupneti, S., Presti, R. M., et al. (2021) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofab483 · Cited by 45
Self-citationFundamental Neurochemistry Review: Microglial immunometabolism in traumatic brain injury
Strogulski, N. R., Portela, L. V., Polster, B. M., & Loane, D. J. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15959 · Cited by 49
Trained Immunity Confers Prolonged Protection From Listeriosis
Théroude, C., Reverte, M., Heinonen, T., Ciarlo, E., Schrijver, I. T., Antonakos, N., Maillard, N., Pralong, F. P., Roy, D. L., & Roger, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.723393 · Cited by 45
Lung, T. W. F., Chan, L. C., Prince, A. S., Yeaman, M. R., Archer, N. K., Aman, M. J., & Proctor, R. A. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1060810 · Cited by 46
Contributions of Inflammation to Cardiometabolic Heart Failure with Preserved Ejection Fraction
Thorp, E. B., & Filipp, M. E. (2024) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-111523-023405 · Cited by 47
Immunometabolic approaches to prevent, detect, and treat neonatal sepsis
Conti, M. G., Angelidou, A., Diray‐Arce, J., Smolen, K. K., Lasky-Su, J. A., Curtis, M. D., & Levy, O. (2019) · Pediatric Research · doi:10.1038/s41390-019-0647-6 · Cited by 46
Oat-Derived β-Glucans Induced Trained Immunity Through Metabolic Reprogramming
Pan, W. X., Hao, S., Zheng, M., Lin, D., Jiang, P., Zhao, J., Shi, H., Yang, X., Li, X., & Yu, Y. (2020) · Inflammation · doi:10.1007/s10753-020-01211-2 · Cited by 44
Reversing Post-Infectious Epigenetic-Mediated Immune Suppression
Abhimanyu, A., Ontiveros, C. O., Guerra-Resendez, R. S., Nishiguchi, T., Ladki, M., Hilton, I. B., Schlesinger, L. S., & DiNardo, A. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.688132 · Cited by 46
Zhou, J., Lv, J., Carlson, C., Liu, H., Wang, H., Xu, T., Wu, F., Song, C., Wang, X., Wang, T., et al. (2021) · Emerging Microbes & Infections · doi:10.1080/22221751.2021.1899771 · Cited by 44
Acevedo, O. A., Berríos-Rojas, R. V., Rodríguez‐Guilarte, L., Lillo-Dapremont, B., & Kalergis, A. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.745332 · Cited by 45
Two Faces of Macrophages: Training and Tolerance
Zubair, K., You, C., Kwon, G., & Kang, K. (2021) · Biomedicines · doi:10.3390/biomedicines9111596 · Cited by 47
Diverse Epigenetic Regulations of Macrophages in Atherosclerosis
Yang, H., Sun, Y., Li, Q., Jin, F., & Dai, Y. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.868788 · Cited by 46
The effect of influenza vaccination on trained immunity: impact on COVID-19Preprint
Debisarun, P. A., Struycken, P., Domínguez‐Andrés, J., Moorlag, S. J. C. F. M., Taks, E., Gössling, K. L., Ostermann, P. N., Müller, L., Schaal, H., ten Oever, J., et al. (2020) · medRxiv · doi:10.1101/2020.10.14.20212498 · Cited by 45
Self-citationGoretzki, A., Lin, Y., & Schülke, S. (2021) · Allergy · doi:10.1111/all.14843 · Cited by 42
Karakike, E., Scicluna, B. P., Roumpoutsou, M., Mitrou, I., Karampela, N., Karageorgos, A., Psaroulis, K., Massa, E., Pitsoulis, A., Chaloulis, P., et al. (2022) · Critical Care · doi:10.1186/s13054-022-04055-4 · Cited by 42
Sander, L. E., & Garaude, J. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.10.008 · Cited by 41
Memory-Like Responses of Brain Microglia Are Controlled by Developmental State and Pathogen Dose
Lajqi, T., Stojiljkovic, M. R., Williams, D. L., Hudalla, H., Bauer, M. W., Witte, O. W., Wetzker, R., Bauer, R., & Schmeer, C. W. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.546415 · Cited by 41
Self-citationFatty acid desaturation and lipoxygenase pathways support trained immunity
Ferreira, A. V., Alarcon-Barrera, J. C., Domínguez‐Andrés, J., Bulut, O. P., Kılıç, G., Debisarun, P. A., Röring, R. J., Özhan, H. N., Terschlüsen, E., Ziogas, A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43315-x · Cited by 43
Self-citationInnate Immune Function of Mitochondrial Metabolism
Sancho, D., Enamorado, M., & Garaude, J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00527 · Cited by 40
Metadata
- Authors
- Arts, R. J. W., Novakovic, B., ter Horst, R., Carvalho, A., Bekkering, S., Lachmandas, E., Rodrigues, F., Silvestre, R., Cheng, S.-C., Wang, S.-Y., Habibi, E., Gonçalves, L. G., Mesquita, I., Cunha, C., van Laarhoven, A., van de Veerdonk, F. L., Williams, D. L., van der Meer, J. W. M., Logie, C., O'Neill, L. A., Dinarello, C. A., Riksen, N. P., van Crevel, R., Clish, C., Notebaart, R. A., Joosten, L. A. B., Stunnenberg, H. G., Xavier, R. J., & Netea, M. G.
- Affiliations
- Radboud University Medical Center (NL)
- Radboud University Nijmegen (NL)
- University of Minho (PT)
- National Tsing Hua University (TW)
- Instituto de Tecnologia Química e Biológica António Xavier (PT)
- East Tennessee State University (US)
- Trinity College Dublin (IE)
- Broad Institute (US)
- Corresponding author
- Arts, Rob J.W.
- ORCID
- Arts, Rob J.W.
- Novakovic, Boris
- Carvalho, Agostinho
- Bekkering, Siroon
- Rodrigues, Fernando
- Silvestre, Ricardo
- Cheng, Shih-Chin
- Wang, Shuang-Yin
- Habibi, Ehsan
- Gonçalves, Luís G.
- Mesquita, Inês
- Cunha, Cristina
- Williams, David L.
- Logie, Colin
- O'Neill, Luke A.
- Dinarello, Charles A.
- Riksen, Niels P.
- Clish, Clary
- Notebaart, Richard A.
- Joosten, Leo A.B.
- Stunnenberg, Hendrik G.
- Xavier, Ramnik J.
- Netea, Mihai G.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 24
- Issue
- 6
- Pages
- 807-819
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC5742541
- OpenAlex
- W2557169014
- Cited by
- 930
- References
- 42
- Citations by year
- 2026: 134 · 2025: 120 · 2024: 101 · 2023: 81 · 2022: 118 · 2021: 111 · 2020: 108 · 2019: 66 · 2018: 62 · 2017: 28 · 2016: 1
- FWCI
- 31.71
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Socio-Environmental Systems Modeling (acceptedVersion, cc-by-nc-nd)
- Digital Commons - East Tennessee State University (East Tennessee State University) (submittedVersion, cc-by-nc-nd)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, cc-by-nc-nd)
- Radboud Repository (Radboud University) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion, cc-by-nc-nd)
- Funders
- ERC Consolidator (310372)
- Spinoza
- Netherlands Organization for Scientific Research
- NHMRC
- CJ Martin Early Career Fellowship
- Dr. Dekker
- Netherlands Heart Foundation (2012T051)
- H2020
- European Union (667837)
- Fundação para a Ciência e Tecnologia (IF/00735/2014, IF/00021/2014, RECI/BBB-BQB/0230/2012, SFRH/BPD/96176/2013)
- FCT (RECI/BBB-BQB/0230/2012)
- Programa Operacional Regional do Norte (ON.2—O Novo Norte)
- Quadro de Referência Estratégico Nacional
- Fundo Europeu de Desenvolvimento Regional
- Projeto Estratégico (LA 26 – 2013–2014 (PEst-C/SAU/LA0026/2013)
- NIH (DK43351, DK097485, GM53522, GM083016, GM119197, C06RR0306551)
- Helmsley Trust
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- trained immunity, glutaminolysis, fumarate accumulation, monocytes, β-glucan, epigenetic reprogramming, cholesterol biosynthesis, glycolysis, TCA cycle, immunometabolism, epigenetic rewiring
- MeSH terms
- Cholesterol, Fumarates, Glucose, Glutamine, Glycolysis, Humans, Immune Tolerance, Immunity, Innate, Macrophages, Models, Biological, Pentose Phosphate Pathway, Epigenesis, Genetic, Hypoxia-Inducible Factor 1, alpha Subunit, Proteolysis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review